CNR Institutional Research Information System

LIGUORI, MARIA
 Distribuzione geografica
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Continente #
AS - Asia 3.876
NA - Nord America 1.786
EU - Europa 845
SA - Sud America 610
Continente sconosciuto - Info sul continente non disponibili 158
AF - Africa 67
OC - Oceania 8
Totale 7.350
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Nazione #
US - Stati Uniti d'America 1.683
SG - Singapore 1.496
CN - Cina 969
BR - Brasile 514
HK - Hong Kong 400
VN - Vietnam 371
IT - Italia 287
FR - Francia 224
KR - Corea 184
JP - Giappone 180
NL - Olanda 111
IN - India 64
BD - Bangladesh 51
AR - Argentina 40
CA - Canada 38
DE - Germania 36
GB - Regno Unito 34
FI - Finlandia 33
IL - Israele 28
ID - Indonesia 27
EC - Ecuador 21
IQ - Iraq 21
ZA - Sudafrica 20
ES - Italia 15
SE - Svezia 13
JM - Giamaica 12
MA - Marocco 12
MX - Messico 12
TR - Turchia 12
AT - Austria 11
PL - Polonia 11
CO - Colombia 10
TN - Tunisia 10
UA - Ucraina 10
CL - Cile 9
CR - Costa Rica 9
KE - Kenya 9
UZ - Uzbekistan 9
IE - Irlanda 8
PH - Filippine 8
RU - Federazione Russa 8
AU - Australia 7
SA - Arabia Saudita 7
PK - Pakistan 6
VE - Venezuela 6
AE - Emirati Arabi Uniti 5
MY - Malesia 5
PE - Perù 5
PT - Portogallo 5
TT - Trinidad e Tobago 5
AZ - Azerbaigian 4
BB - Barbados 4
DO - Repubblica Dominicana 4
DZ - Algeria 4
HN - Honduras 4
KG - Kirghizistan 4
KZ - Kazakistan 4
NI - Nicaragua 4
SK - Slovacchia (Repubblica Slovacca) 4
TH - Thailandia 4
GR - Grecia 3
LT - Lituania 3
NP - Nepal 3
PR - Porto Rico 3
PY - Paraguay 3
AL - Albania 2
BA - Bosnia-Erzegovina 2
BE - Belgio 2
BO - Bolivia 2
BZ - Belize 2
CZ - Repubblica Ceca 2
DK - Danimarca 2
EE - Estonia 2
HU - Ungheria 2
IR - Iran 2
JO - Giordania 2
MD - Moldavia 2
MT - Malta 2
SC - Seychelles 2
SV - El Salvador 2
SY - Repubblica araba siriana 2
TW - Taiwan 2
BF - Burkina Faso 1
BG - Bulgaria 1
BQ - ???statistics.table.value.countryCode.BQ??? 1
BS - Bahamas 1
BY - Bielorussia 1
CG - Congo 1
CH - Svizzera 1
CI - Costa d'Avorio 1
EG - Egitto 1
HR - Croazia 1
IM - Isola di Man 1
KW - Kuwait 1
LB - Libano 1
LK - Sri Lanka 1
LU - Lussemburgo 1
LV - Lettonia 1
MK - Macedonia 1
MM - Myanmar 1
Totale 7.178
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Città #
Singapore 881
Santa Clara 581
Hefei 486
Hong Kong 394
San Jose 227
Seoul 183
Lauterbourg 171
Tokyo 149
Ho Chi Minh City 146
Beijing 144
Ashburn 106
Dallas 91
Hanoi 74
Los Angeles 71
São Paulo 41
Rome 36
New York 31
Minamishinagawa 27
Buffalo 26
Helsinki 25
Milan 22
Da Nang 20
Bengaluru 17
Rio de Janeiro 16
Haiphong 15
Bari 12
Brasília 12
Brooklyn 12
Frankfurt am Main 11
Porto Alegre 11
Amsterdam 10
Belo Horizonte 10
Genoa 10
Guarulhos 10
Orem 10
Toronto 10
Campinas 9
Cape Town 9
Chicago 9
Curitiba 9
Dhaka 9
Tashkent 9
Turin 9
Atlanta 8
Barcellona Pozzo di Gotto 8
Florence 8
Fortaleza 8
Ha Long 8
Montreal 8
Nairobi 8
Naples 8
Nuremberg 8
Surabaya 8
The Bronx 8
Thái Bình 8
Anoia Superiore 7
Baghdad 7
Biên Hòa 7
Boardman 7
Dublin 7
Guangzhou 7
Kingston 7
Milwaukee 7
Quito 7
San José 7
Warsaw 7
Bologna 6
Buenos Aires 6
Cabo Frio 6
Can Tho 6
Catania 6
Guayaquil 6
Johannesburg 6
London 6
Manaus 6
Potenza 6
Quận Bình Thạnh 6
Salvador 6
Santo André 6
Stockholm 6
Sydney 6
Tunis 6
Washington 6
Boston 5
Charlotte 5
Chennai 5
Figino 5
Houston 5
Lappeenranta 5
Las Vegas 5
Manchester 5
New Delhi 5
Philadelphia 5
Portsmouth 5
Queens 5
Shanghai 5
São Bernardo do Campo 5
Vienna 5
Assago 4
Baku 4
Totale 4.519
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Nome #
Tay Sachs in South Italy 165
An early Transcriptomic Investigation in Adult Patients with Spinal Muscular Atrophy Under Treatment with Nusinersen 108
MicroRNA and transcription factor co-regulatory network analysis: a combined bioinformatics and molecular strategy for uncovering genetic hub regulatory elements in multiple sclerosis pathogenesis 98
Sex and Gender Differences in Neurodegenerative Diseases: Challenges for Therapeutic Opportunities 95
A Pilot Longitudinal Evaluation of MicroRNAs for Monitoring the Cognitive Impairment in Pediatric Multiple Sclerosis 93
Medicina di Precisione in Pediatria - Biotecnologie e applicazioni per lo sviluppo e la salute 93
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis 86
Associazione tra la subunità 2B del recettore NMDA (gene GRIN2B) e la malattia di Alzheimer 85
Impact of individual cognitive profile on visuo-motor reorganization in relapsing-remitting multiple sclerosis 84
Counting of peripheral extracellular vesicles in Multiple Sclerosis patients by an improved nanoplasmonic assay and dynamic light scattering 83
Investigating the Role of MicroRNA and Transcription Factor Co-regulatory Networks in Multiple Sclerosis Pathogenesis 82
Mutational screening of the eIF2B5 gene in sib pairs affected by multiple sclerosis. 80
Conventional MRI and NOTCH3 gene screening in sporadic CADASIL. 77
Treating epilepsy in Italy between XIX and XX century 76
Functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis 75
Neuropsychological impact on motor reorganization in relapsing remitting multiple sclerosis 72
Investigation of the relationship between anti-GM1 antibodies and brain atrophy in multiple sclerosis 67
Two Novel Cysteine-Sparing Notch3 Mutations In Patients With CADASIL 67
The effects of BDNF Val(66)Met polymorphism on brain function in controls and patients with multiple sclerosis: An imaging genetic study. 66
A novel missense mutation (p.Arg309His) in the nuclear localization signal sequence of spastin protein causes a complicated form of Hereditary Spastic Paraplegia 66
Glutamate and multiple sclerosis. 66
Association between miRNAs expression and cognitive performances of Pediatric Multiple Sclerosis patients: A pilot study 65
Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype 63
Meta-Analysis of Differential Connectivity in Gene Co-Expression Networks in Multiple Sclerosis 63
Apolipoprotein E genotype does not influence the progression of multiple sclerosis. 60
First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia. 60
A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease. 58
A Predictive Model for MicroRNA Expressions in Pediatric Multiple Sclerosis Detection 58
Changes of serum sICAM-1 and MMP-9 induced by rIFNbeta-1b treatment in relapsing-remitting MS 57
Molecular signatures associated with cognitive dysfunctions in pediatric multiple sclerosis 57
CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY 55
Investigating the Role of MicroRNA and Transcription Factor Co-regulatory Networks in Multiple Sclerosis Pathogenesis 54
Molecular Characterization of Peripheral Extracellular Vesicles in Clinically Isolated Syndrome: Preliminary Suggestions from a Pilot Study. 54
Gene symbol: NOTCH3 53
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy 53
Combined microRNA and mRNA expression analysis in pediatric multiple sclerosis: an integrated approach to uncover novel pathogenic mechanisms of the disease. 53
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. 51
An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis Patients 50
Dysregulation of MicroRNAs and Target Genes Networks in Peripheral Blood of Patients With Sporadic Amyotrophic Lateral Sclerosis 50
Identification of a patient affected by "Juvenile-chronic" Tay Sachs disease in South Italy. 50
Axonal damage in multiple sclerosis plaques: a combined magnetic resonance imaging and 1H-magnetic resonance spectroscopy study 48
Cognitive impairment and brain atrophy in patients with relapsing-remitting Multiple Sclerosis (RRMS): the role of brain derived neurotrophic factor (BDNF) gene. 48
CSF MALDI-TOF mass spectrometry protein profiling in Clinically Isolated Syndrome. 48
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 48
Peripheral mRNA expression of brain-derived neurotrophic factor Val66Met polymorphism in patients with relapsing-remitting multiple sclerosis 48
Age at onset in multiple sclerosis 46
COGNITIVE DYSFUNCTION AND QUALITY OF LIFE IN MULTIPLE SCLEROSIS DISEASE 46
Fas antigen and sporadic Alzheimer's disease in Southern Italy:evaluation of two polymorphisms in the TNFRSF6 gene. 45
Mutation analysis of the GRIN2B gene in Alzheimer's disease 45
Impact of individual cognitive profile on visuo-motor reorganization in relapsing-remitting multiple sclerosis 45
Brain-Derived Neurotrophic Factor Val66Met polymorphism and peripheral mrna expression in patients with Relapsing Remitting Multiple Sclerosis (RRMS). 44
The influence of age at onset on the course of multiple sclerosis 44
Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis 43
Visualizing genetic influences on Human brain function: Interactive effects of BNDF and COMT allelic variations on a spatial working memory network 42
Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia 42
Listening to the neurological teams for multiple sclerosis: the SMART project 42
Gly269Ser mutation in compound heterozygosity with Leu127Arg is associated with adult onset of Tay-Sachs: a case report from south Italy 41
ADULT ONSET TAY-SACHS ASSOCIATED WITH -HEXOSAMINIDASE A DEFICIENCY: A CASE REPORT FROM SOUTH ITALY 41
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease 41
Proteomic profiling in multiple sclerosis clinical courses reveals potential biomarkers of neurodegeneration 41
Course and prognosis in early-onset MS: comparison with adult-onset forms. 40
D678N mutation in a patient with an early-onset Alzheimer's Disease 40
Ventro-Lateral Prefrontal activity during working-memory processing is modulated by Monoamine oxidase-A genetic variation 40
Polymorphisms and mutational analysis of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 39
Neuropatia ottica ereditaria di Leber s e Sclerosi Multipla: Harding s syndrome. 39
Impact of brain atrophy and cognitive profile on visuo-motor reorganization in relapsing-remitting multiple sclerosis 39
Neurofunctional correlates of personality traits in relapsing-remitting multiple sclerosis: an fMRI study. 39
BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS): LONGITUDINAL EVALUATION 38
PERIPHERAL MRNA EXPRESSION OF BRAIN-DERIVED NEUROTROPHIC FACTOR VAL66MET POLYMORPHISM IN PATIENTS WITH RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS). 38
SERUM AND CSF ANTI-GM1 ANTIBODIES IN PATIENTS WITH GUILLAIN-BARRE-SYNDROME AND CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY 38
Preliminary evidences of a NOS2A protective effect from Relapsing-Remitting Multiple Sclerosis 37
Assenza di correlazione tra sclerosi multipla familiare (SM) e mutazioni nel gene eIF2B5. 37
APP gene mutation (D678N) in a patient with an Early-Onset Alzheimer's Disease 37
Familial Alzheimer's disease with amyloid precursor protein D678N mutation: a case report 37
PROGRESSION OF MOBILITY IMPAIRMENT AND BRAIN WHITE MATTER LESION VOLUME IN THE ELDERLY: A TWO-YEAR LONGITUDINAL STUDY 36
The role of mri in the NOTCH3 gene screening of apparently sporadic CADASIL 36
High resolution proton MR spectroscopy of cerebrospinal fluid in MS patients. Comparison with biochemical changes in demyelinating plaques 36
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes 36
A phenotyphic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. 36
Brain-derived Neurotrophic Factor Val66Met polimorphism and the cortical response to spatial working memory. 36
Brain-derived neurotrophic factor and risk for primary adult-onset cranial-cervical dystonia 35
CADASIL: extended polymorphisms and mutational analysis of the NOTCH3 gene. 35
Serum prolactin concentrations in patients with multiple sclerosis 35
Neuropsychological influence on motor reorganization in relapsing remitting MS patients 35
An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population 34
Screening for MELAS mutations in Italian patients having stroke-like episodes. 34
Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification 34
Anti-GM1 antibodies are not associated with cerebral atrophy in patients with multiple sclerosis. 34
Depression and Parkinson's disease:a neuropsychological view 33
Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis 33
CADASIL: molecular screening of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 33
CA repeat estrogen receptor b gene polymorphism in patients with Multiple Sclerosis. 33
Preliminary evidences of a NOS2A protective effect from relapsing-remitting multiple sclerosis. 32
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 32
Trauma cranico e genotipo APO-E: causa o rischio di malatia di Alzheimer? 32
DISTINGUISHING APPARENTLY SPORADIC CADASIL FROM OTHER LEUCOENCEPHALOPATHIES:THE ROLE OF MAGNETIC RESONANCE IMAGING IN THE NOTCH3 GENE SCREENING 31
Brain-derived neurotrophic factor val66met polymorphysm and the cortical response to spatial working memory 31
Dysregulation of Gene Expressions in Multiple Sclerosis: TNFSF13B and Other Candidate Genes 31
Evidence for early grey matter involvement in adaptive cortical change of dorsal premotor cortex in relapsing remitting multiple sclerosis 31
Genetic screening of Alzheimer's disease genes in Italian samples yields novel mutations in Presenilin-enhancer 2. 30
Totale 5.148
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Categoria #
all - tutte 25.182
article - articoli 15.073
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 197
Totale 40.452
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202472 0 0 0 0 0 0 0 0 49 0 18 5
2024/20252.657 7 17 181 105 645 51 37 83 56 162 686 627
2025/20264.367 265 496 489 623 689 194 623 229 332 240 104 83
2026/2027254 249 5 0 0 0 0 0 0 0 0 0 0
Totale 7.350